Canonical Allele Identifier: CA2628329616

Gene: FBN1

Linked Data

• gnomAD v4: 15-48421871-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421871T>C , CM000677.2:g.48421871T>C	GRCh38
NC_000015.9:g.48714068T>C , CM000677.1:g.48714068T>C	GRCh37
NC_000015.8:g.46501360T>C	NCBI36
NG_008805.2:g.228918A>G , LRG_778:g.228918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*378+81A>G	ENSP00000453958.2:n.*378+81A>G
ENST00000674301.2:c.*1083+81A>G	ENSP00000501333.2:n.*1083+81A>G
ENST00000682170.1:n.1751+81A>G
ENST00000682767.1:n.867+81A>G
ENST00000316623.10:c.7570+81A>G MANE Select	ENSP00000325527.5:n.7570+81A>G
ENST00000674301.1:c.2736+81A>G	ENSP00000501333.1:n.2736+81A>G
ENST00000316623.9:c.7570+81A>G	ENSP00000325527.5:n.7570+81A>G
ENST00000559133.5:c.2939+81A>G
NM_000138.4:c.7570+81A>G , LRG_778t1:c.7570+81A>G	NP_000129.3:n.7570+81A>G
NM_000138.5:c.7570+81A>G MANE Select	NP_000129.3:n.7570+81A>G